Clinical practice guidelines: management of Pulmonary Arterial Hypertension (PAH). Manual. Health Technology Assessment Unit, Putrajaya, Malaysia. (2011)
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Abstract
Pulmonary arterial hypertension (PAH) is defined as a group of diseases characterized by a progressive increase of pulmonary vascular resistance (PVR) leading to right ventricular failure and premature death. Untreated, it is a potentially devastating disease. However, the past decade has seen remarkable improvements in our understanding of the pathology associated with the condition and the development of PAH-specific therapies with the ability to alter the natural history of the disease.
Item Type: | Monograph (Manual) |
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Keywords: | Pulmonary arterial hypertension, Pulmonary hypertension, Heart failure, Cardiology |
Taxonomy: | By Subject > Health Sciences > Nursing |
Local Content Hub: | Subjects > Health Sciences |
Depositing User: | Farleen Azrina Zamberi |
Date Deposited: | 04 Jul 2022 03:04 |
Last Modified: | 04 Jul 2022 03:04 |
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